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在 DNA 梳状实验中同时可视化 R 环/RNA:DNA 杂交体和复制叉。

Simultaneous Visualization of R-Loops/RNA:DNA Hybrids and Replication Forks in a DNA Combing Assay.

机构信息

Early Oncology Bioscience, AstraZeneca, Cambridge CB2 0AA, UK.

The Francis Crick Institute, London NW1 1AT, UK.

出版信息

Genes (Basel). 2024 Sep 3;15(9):1161. doi: 10.3390/genes15091161.

Abstract

R-loops, structures that play a crucial role in various biological processes, are integral to gene expression, the maintenance of genome stability, and the formation of epigenomic signatures. When these R-loops are deregulated, they can contribute to the development of serious health conditions, including cancer and neurodegenerative diseases. The detection of R-loops is a complex process that involves several approaches. These include S9.6 antibody- or RNAse H-based immunoprecipitation, non-denaturing bisulfite footprinting, gel electrophoresis, and electron microscopy. Each of these methods offers unique insights into the nature and behavior of R-loops. In our study, we introduce a novel protocol that has been developed based on a single-molecule DNA combing assay. This innovative approach allows for the direct and simultaneous visualization of RNA:DNA hybrids and replication forks, providing a more comprehensive understanding of these structures. Our findings confirm the transcriptional origin of the hybrids, adding to the body of knowledge about their formation. Furthermore, we demonstrate that these hybrids have an inhibitory effect on the progression of replication forks, highlighting their potential impact on DNA replication and cellular function.

摘要

R 环是在各种生物过程中发挥关键作用的结构,是基因表达、基因组稳定性维持和表观基因组特征形成的组成部分。当这些 R 环失调时,它们可能导致严重的健康状况的发展,包括癌症和神经退行性疾病。R 环的检测是一个复杂的过程,涉及几种方法。这些方法包括 S9.6 抗体或 RNAse H 为基础的免疫沉淀、非变性亚硫酸氢盐足迹分析、凝胶电泳和电子显微镜。这些方法中的每一种都提供了对 R 环的性质和行为的独特见解。在我们的研究中,我们引入了一种基于单分子 DNA 梳理分析的新方案。这种创新方法允许直接和同时可视化 RNA:DNA 杂交体和复制叉,从而更全面地了解这些结构。我们的发现证实了杂交体的转录起源,增加了对其形成的了解。此外,我们证明这些杂交体对复制叉的推进有抑制作用,突出了它们对 DNA 复制和细胞功能的潜在影响。

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